#MHRA

top of page

Home
Services
Contact Us
Meet the Team
FAQ's
News
More

Use tab to navigate through the menu items.

ECTD Pharma News

All Posts

Search

Key 2025–2026 Events for Regulatory Services Professionals

Key 2025–2026 Events for Regulatory Services Professionals

Key 2025–2026 Events for Regulatory Services Professionals

Are you offering regulatory services—like eCTD publishing, pharmacovigilance, or MHRA/EMA support? These global events are essential to...

Jun 124 min read

Find Us

Tel: +447506975972 & +447734219260

ectdpharma@outlook.com

Cheryl.Allen@ectdpharma.com

Thomas.Marsden@ectdpharma.com

Offices based in London & Nottingham, United Kingdom

EMEA

MHRA

FDA

swissmedic

Health CA

Regulatory Submission Services | eCTD Publishing Experts – eCTD Pharma
At eCTD Pharma, we deliver industry-leading regulatory submission services tailored for the pharmaceutical, biotech, and healthcare sectors. Our expertise in eCTD publishing, regulatory gap analysis, and legacy submission conversions ensures your submissions are 100% compliant with EMA, FDA, and global health authority standards. Using advanced Freyr software, we provide fast, accurate, and secure electronic submissions, reducing approval timelines and minimizing compliance risks. Whether you need end-to-end eCTD submission support, lifecycle management, or expert consultancy, eCTD Pharma is your trusted partner. Maximize compliance. Minimize delays. Accelerate approvals. Contact eCTD Pharma today to streamline your regulatory process.

bottom of page